NL-OMON32532已完成不适用
Clinical feasibility and performance of a continuous finger blood pressure measurement device in the perioperative period - Nexfin study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 111
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Group A (Patients undergoing cardiothoracic surgery)
- •* Patients undergoing elective cardiothoracic surgery
- •* Use of a pulmonary artery catheter (PAC)
- •* Age 18-75 years
- •* Maximal ICU stay of 24 hours
- •* Informed consent
- •Group B (Volunteers)
- •* Healthy subjects
- •* Age 18-50 years
- •* Informed consent
- •Group C (Patients undergoing elective abdominal surgery)
- •* Patients undergoing elective abdominal surgery
- •* Age 18-75 years
- •* Informed consent
排除标准
- •Group A (Patients undergoing cardiothoracic surgery)
- •* Emergency operation
- •* Body mass index (BMI) 15 < BSA > 35
- •* Diabetes mellitus
- •Group B (Volunteers)
- •* Body mass index (BMI) 15 < BSA > 35
- •* Underlying cardiovascular diseases
- •* Use of beta blockers or anti-hypertensive drugs
- •* Use of diuretics
- •* Diabetes mellitus
- •* Use of coffee or cigarettes before the measurements take place
- •Group C (Patients undergoing elective abdominal surgery)
- •* Body mass index (BMI) 15 < BSA > 35
- •* Use of beta blockers or anti-hypertensive drugs
- •* Use of diuretics
- •* Diabetes mellitus
研究者
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